In-line vessel sealer and divider

ABSTRACT

An endoscopic forceps includes a housing having a shaft attached thereto, the shaft including a pair of jaw members disposed at a distal end thereof. The forceps also includes a drive assembly disposed in the housing which moves the jaw members relative to one another from a first position wherein the jaw members are disposed in spaced relation relative to one another to a second position wherein the jaw members are closer to one another for manipulating tissue. A pair of handles is operatively connected to the drive assembly and the handles are movable relative to the housing to actuate the drive assembly to move the jaw members. Each of the jaw members is adapted to connect to a source of electrical energy such that the jaw members are capable of conducting energy for treating tissue. The forceps also includes a first switch disposed on the housing which is activatable to selectively deliver energy of a first electrical potential to at least one jaw member for treating tissue in a monopolar fashion. A second switch is disposed on the housing and is activatable to selectively deliver energy of a first electrical potential to one jaw member and selectively deliver energy of a second electrical potential to the other jaw member for treating tissue in a bipolar fashion.

CROSS REFERENCE TO RELATED APPLICATION

This application is a continuation-in-part of U.S. application Ser. No. 11/540,335, filed Sep. 29, 2006 entitled “IN-LINE VESSEL SEALER AND DIVIDER” by Dumbauld et al. which claims the benefit of priority to U.S. Provisional Application Ser. No. 60/722,177 filed Sep. 30, 2005 entitled “IN-LINE VESSEL SEALER AND DIVIDER” by Patrick L. Dumbauld, the entire contents of which being incorporated by reference herein.

BACKGROUND

The present disclosure relates to an electrosurgical forceps and more particularly, the present disclosure relates to an elongated endoscopic combination bipolar and monopolar electrosurgical forceps for sealing and/or cutting tissue.

TECHNICAL FIELD

Electrosurgical forceps utilize both mechanical clamping action and electrical energy to affect hemostasis by heating tissue and blood vessels to coagulate, cauterize and/or seal tissue. As an alternative to open forceps for use with open surgical procedures, many modern surgeons use endoscopes and endoscopic instruments for remotely accessing organs through smaller, puncture-like incisions. As a direct result thereof, patients tend to benefit from less scarring and reduced healing time.

Endoscopic instruments are inserted into the patient through a cannula, or port, which has been made with a trocar. Typical sizes for cannulas range from three millimeters to twelve millimeters. Smaller cannulas are usually preferred, which, as can be appreciated, ultimately presents a design challenge to instrument manufacturers who must find ways to make endoscopic instruments that fit through the smaller cannulas.

Many endoscopic surgical procedures require cutting or ligating blood vessels or vascular tissue. Due to the inherent spatial considerations of the surgical cavity, surgeons often have difficulty suturing vessels or performing other traditional methods of controlling bleeding, e.g., clamping and/or tying-off transected blood vessels. By utilizing an endoscopic electrosurgical forceps, a surgeon can either cauterize, coagulate/desiccate and/or simply reduce or slow bleeding simply by controlling the intensity, frequency and duration of the electrosurgical energy applied through the jaw members to the tissue. Most small blood vessels, i.e., in the range below two millimeters in diameter, can often be closed using standard electrosurgical instruments and techniques. However, if a larger vessel is ligated, it may be necessary for the surgeon to convert the endoscopic procedure into an open-surgical procedure and thereby abandon the benefits of endoscopic surgery. Alternatively, the surgeon can seal the larger vessel or tissue.

It is thought that the process of coagulating vessels is fundamentally different than electrosurgical vessel sealing. For the purposes herein, “coagulation” is defined as a process of desiccating tissue wherein the tissue cells are ruptured and dried. “Vessel sealing” or “tissue sealing” is defined as the process of liquefying the collagen in the tissue so that it reforms into a fused mass. Coagulation of small vessels is sufficient to permanently close them, while larger vessels need to be sealed to assure permanent closure.

In order to effectively seal larger vessels (or tissue) two predominant mechanical parameters must be accurately controlled - the pressure applied to the vessel (tissue) and the gap distance between the electrodes or tissue sealing surfaces—both of which are affected by the thickness of the sealed vessel. More particularly, accurate application of pressure is important to oppose the walls of the vessel; to reduce the tissue impedance to a low enough value that allows enough electrosurgical energy through the tissue; to overcome the forces of expansion during tissue heating; and to contribute to the end tissue thickness which is an indication of a good seal. It has been determined that a typical jaw gap for fusing vessel walls is optimum between 0.001 and 0.006 inches. Below this range, the seal may shred or tear and above this range the lumens may not be properly or effectively sealed.

With respect to smaller vessels, the pressure applied to the tissue tends to become less relevant whereas the gap distance between the electrically conductive surfaces becomes more significant for effective sealing. In other words, the chances of the two electrically conductive surfaces touching during activation increases as vessels become smaller.

Many known instruments include blade members or shearing members which simply cut tissue in a mechanical and/or electromechanical manner and are relatively ineffective for vessel sealing purposes. Other instruments rely on clamping pressure alone to procure proper sealing thickness and are not designed to take into account gap tolerances and/or parallelism and flatness requirements which are parameters which, if properly controlled, can assure a consistent and effective tissue seal. For example, it is known that it is difficult to adequately control thickness of the resulting sealed tissue by controlling clamping pressure alone for either of two reasons: 1) if too much force is applied, there is a possibility that the two poles will touch and energy will not be transferred through the tissue resulting in an ineffective seal; or 2) if too low a force is applied the tissue may pre-maturely move prior to activation and sealing and/or a thicker, less reliable seal may be created.

As mentioned above, in order to properly and effectively seal larger vessels or tissue, a greater closure force between opposing jaw members is required. It is known that a large closure force between the jaws typically requires large actuation forces which are necessary to create a large moment about the pivot for each jaw. This presents a design challenge for instrument manufacturers who must weigh the advantages of manufacturing an overly-simplified design against the disadvantages of a design that may require the user to exert a large closure force to effectively seal tissue. As a result, designers must compensate for these large closure forces by either designing instruments with metal pins and/or by designing instruments which at least partially offload these closure forces to reduce the chances of mechanical failure and reduce fatigue for the end user (i.e., surgeon).

Increasing the closure forces between electrodes may have other undesirable effects, e.g., it may cause the opposing electrodes to come into close contact with one another which may result in a short circuit and a small closure force may cause pre-mature movement of the tissue during compression and prior to activation. As a result thereof, providing an instrument which consistently provides the appropriate closure force between opposing electrode within a preferred pressure range will enhance the chances of a successful seal. As can be appreciated, relying on a surgeon to manually provide the appropriate closure force within the appropriate range on a consistent basis would be difficult and the resultant effectiveness and quality of the seal may vary. Moreover, the overall success of creating an effective tissue seal is greatly reliant upon the user's expertise, vision, dexterity, and experience in judging the appropriate closure force to uniformly, consistently and effectively seal the vessel. In other words, the success of the seal would greatly depend upon the ultimate skill of the surgeon rather than the efficiency of the instrument.

It has been found that the pressure range for assuring a consistent and effective seal is between about 3 kg/cm² to about 16 kg/cm² and, preferably, within a working range of 7 kg/cm² to 13 kg/cm². Manufacturing an instrument which is capable of providing a closure pressure within this working range has been shown to be effective for sealing arteries, tissues and other vascular bundles.

Various force-actuating assemblies have been developed in the past for providing the appropriate closure forces to effect vessel sealing. For example, one such actuating assembly has been developed by Valleylab, Inc. of Boulder, Colo., a division of Tyco Healthcare LP, for use with Valleylab's vessel sealing and dividing instrument commonly sold under the trademark LIGASURE ATLAS®. This assembly includes a four-bar mechanical linkage, a spring and a drive assembly which cooperate to consistently provide and maintain tissue pressures within the above working ranges. Co-pending U.S. application Ser. No. 10/179,863 entitled “VESSEL SEALER AND DIVIDER” (now U.S. Pat. No. 7,101,371), U.S. application Ser. No. 10/116,944 entitled “VESSEL SEALER AND DIVIDER” (now U.S. Pat. No. 7,083,618), U.S. application Ser. No. 10/472,295 entitled “VESSEL SEALER AND DIVIDER” (now U.S. Pat. No. 7,101,372) and PCT Application Serial Nos. PCT/US01/01890 entitled “VESSEL SEALER AND DIVIDER and PCT/US01/11340 entitled “VESSEL SEALER AND DIVIDER” all describe in detail various operating features of the LIGASURE ATLAS® and various methods relating thereto. The contents of all of these applications are hereby incorporated by reference herein.

Other force-actuating mechanisms or assemblies are described in commonly-owned U.S. application Ser. No. 10/460,926 entitled “VESSEL SEALER AND DIVIDER FOR USE WITH SMALL TROCARS AND CANNULAS” and U.S. application Ser. No. 10/953,757 entitled “VESSEL SEALER AND DIVIDER HAVING ELONGATED KNIFE STROKE AND SAFETY FOR CUTTING MECHANISM”, the entire contents of both are hereby incorporated by reference herein. As described therein, simpler and more mechanically advantageous actuating and drive assemblies are described therein which facilitate grasping and manipulating vessels and tissue and which reduce user fatigue.

In certain surgical operations, a bipolar forceps is used in combination with a monopolar forceps or monopolar coagulator to treat tissue and control bleeding during the surgery. As such and during the course of a particular operation, a surgeon may be required to substitute a monopolar instrument for the bipolar instrument which would typically involve substitution through the trocar or cannula. As can be appreciated this may occur on more than one occasion over the course of the operation which can be quite time consuming and which may unnecessarily subject the instruments to possible non-sterile environments.

It would be desirous to develop a small, simple and cost effective combination bipolar and monopolar instrument which can be utilized with small cannulas. Moreover, it would be desirous to provide an instrument which includes an easily manipulatable handle and instrument body which includes a mechanically advantageous force-actuating assembly to reduce user fatigue.

SUMMARY

The present disclosure relates to an endoscopic forceps having a housing with a shaft attached thereto, the shaft including a pair of jaw members disposed at a distal end thereof. The forceps also includes a drive assembly disposed in the housing which is configured to move the jaw members relative to one another from a first position wherein the jaw members are disposed in spaced relation relative to one another to a second position wherein the jaw members are closer to one another for manipulating tissue. A pair of handles is operatively connected to the drive assembly and the handles are configured to move relative to the housing to actuate the drive assembly to move the jaw members. Each jaw member is adapted to connect to a source of electrical energy such that the jaw members are capable of conducting energy for treating tissue.

A first switch is disposed on the housing and is activatable to selectively deliver energy of a first electrical potential to at least one jaw member for treating tissue in a monopolar fashion. A second switch is disposed on the housing and is activatable to selectively deliver energy of a first electrical potential to one jaw member and selectively deliver energy of a second electrical potential to the other jaw member for treating tissue in a bipolar fashion.

In one embodiment according to the present disclosure, the forceps also includes a knife assembly which is operatively associated with the housing. The knife assembly is selectively actuatable to advance a knife through tissue disposed between the jaw members when the jaw members are disposed in the second position. In yet another embodiment, at least one of the jaw members may include a monopolar extension which extends beyond the insulative housing of the jaw member to permit delicate dissection of tissue.

In one particularly useful embodiment, at least one of the handles includes a knife lockout which prevents the knife assembly from being actuated when the jaw members are disposed in the second position. The knife lockout mechanism may include a mechanical interface extending from at least one of the handles. The mechanical interface is dimensioned to impede movement of the knife assembly when the handles are disposed in a first (i.e., open) position relative to the housing and the mechanical interface is dimensioned to permit actuation of the knife assembly when the handles are disposed in a second position relative to the housing.

In another embodiment according to the present disclosure, the forceps includes a monopolar lockout which prevents activation of the first switch when the jaw members are disposed in the first position. In one particularly useful embodiment, the monopolar lockout includes a mechanical interface disposed on at least one of the handles which prevents activation of the first switch when the handles are disposed in a first position relative to the housing and permits activation of the first switch when the handles are disposed in a second position relative to the housing. The monopolar lockout may include a pressure activated switch disposed in the housing such that movement of the handles from a first position relative to the housing to a second position relative to the housing closes the pressure activated switch to allow activation of the first switch.

In still yet another embodiment according to the present disclosure, the handles of the forceps are disposed on opposite sides of the housing and are movable from a first, spaced position relative to the housing to a second closer position relative to the housing. The housing may also be configured to include a pair of slits defined on opposite sides of the housing and the handles may be dimensioned to move relative to the housing within the slits. In one particularly useful embodiment, the housing includes a longitudinal axis defined therethrough and the handles are disposed at an angle “a” relative to the longitudinal axis to facilitate handling.

In yet another embodiment according to the present disclosure, an intensity controller is included which regulates the intensity of electrosurgical energy to the forceps during activation. In a particularly useful embodiment, the intensity controller is a slide potentiometer and is operable only in a monopolar mode.

In still another embodiment, the forceps may include an electrical safety which regulates the forceps to operating in either a bipolar fashion or a monopolar fashion during any given time. In a particularly useful embodiment, the first switch and the second switch are independently and exclusively activatable relative to one another.

The present disclosure also relates to an electrosurgical system having an electrosurgical generator and an endoscopic forceps. The forceps includes a housing having a shaft attached thereto with a pair of jaw members disposed at a distal end thereof. The jaw members are adapted to connect to the electrosurgical generator. The forceps also includes a drive assembly disposed in the housing which moves the jaw members relative to one another from a first position wherein the jaw members are disposed in spaced relation relative to one another to a second position wherein the jaw members are closer to one another for manipulating tissue. A pair of handles is operatively connected to the drive assembly to actuate the drive assembly to move the jaw members.

A first switch is disposed on the housing and is activatable to selectively deliver energy of a first electrical potential to at least one jaw member for treating tissue in a monopolar fashion. A second switch is disposed on the housing and is activatable to selectively deliver energy of a first electrical potential to one jaw member and selectively deliver energy of a second electrical potential to the other jaw member for treating tissue in a bipolar fashion.

In one embodiment, the generator includes a control circuit having a safety circuit which permits independent and exclusive activation of the forceps in either a bipolar or monopolar fashion. The safety circuit may be electrical or electromechanical and activated upon movement to the pair of handles relative to the housing. The generator may also include a control circuit having an isolation circuit operably connected to the second switch which regulates the energy to the jaw members while bypassing the second switch to protect the integrity of the second switch from current overload.

The present disclosure also relates to an endoscopic forceps having a housing with a shaft attached thereto. The shaft includes a pair of jaw members disposed at a distal end thereof. Each jaw member is adapted to connect to a source of electrical energy such that the jaw members are capable of conducting energy for treating tissue. A drive assembly is disposed in the housing and is operable to move the jaw members relative to one another from a first position, wherein the jaw members are disposed in spaced relation relative to one another, to a second position, wherein the jaw members are closer to one another, for manipulating tissue. A pair of handles operatively connects to the drive assembly and is movable relative to the housing to actuate the drive assembly to move the jaw members.

A knife assembly is included which is operatively associated with the housing. The knife assembly is selectively actuatable to advance a knife through tissue disposed between the jaw members when the jaw members are disposed in the second position. The knife assembly includes at least one safety mechanism to prevent damaging the knife upon selective actuation thereof.

In one embodiment, the safety mechanism includes a mechanical fuse which fractures upon exertion of excessive force (a force of about 9 lbf or greater) to actuate the knife assembly. In another embodiment, the knife assembly includes a pinion gear interdisposed between a set of gear teeth and a track which cooperate to advance the knife distally through the jaw members. The mechanical fuse may be operatively associated with the pinion gear, gear teeth and/or the track. In one particular embodiment, an axle of the pinion gear is designed to fracture upon excessive force to actuate the knife assembly. In another embodiment according to the present disclosure, first and second switches may be included to deliver energy to the jaw members as described mentioned above.

The present disclosure also relates to an endoscopic forceps having a housing with a shaft attached thereto. The shaft includes a pair of jaw members disposed at a distal end thereof, each jaw member adapted to connect to a source of electrical energy such that the jaw members are capable of conducting energy for treating tissue. A drive assembly is disposed in the housing and is operable to move the jaw members relative to one another from a first position, wherein the jaw members are disposed in spaced relation relative to one another, to a second position, wherein the jaw members are closer to one another, for manipulating tissue. A pair of handles is included which operatively connects to the drive assembly and is movable relative to the housing to actuate the drive assembly to move the jaw members.

A switch is included which is disposed on the housing and is activatable to selectively deliver energy of a first electrical potential to at least one jaw member for treating tissue. The switch is operatively coupled to an intensity control mechanism disposed within the housing which is selectively adjustable to regulate the level of electrosurgical energy to at least one jaw member. In one embodiment, the intensity control mechanism is selectively adjustable in discreet increments. In another embodiment, the intensity control mechanism includes a first mechanical interface (e.g., a detent) configured to engage a series of corresponding mechanical interfaces (e.g., recesses) defined in the housing to regulate the level of electrosurgical energy in discreet increments. The detent may be disposed in a cantilevered fashion atop the intensity control mechanism and the intensity control mechanism may be disposed atop a railway to facilitate movement thereof.

In yet another embodiment, the intensity control mechanism includes a second mechanical interface (e.g., a slide bump) that cooperates with the detent to mechanically engage a circuit board disposed within the housing at discreet locations when the detent engages a corresponding one of the series of recesses.

The present disclosure also relates to an endoscopic forceps having a housing with a shaft attached thereto. The shaft includes a pair of jaw members disposed at a distal end thereof, each jaw member adapted to connect to a source of electrical energy such that the jaw members are capable of conducting energy for treating tissue. A drive assembly is disposed in the housing and is operable to move the jaw members relative to one another from a first position, wherein the jaw members are disposed in spaced relation relative to one another, to a second position, wherein the jaw members are closer to one another, for manipulating tissue. A pair of handles operatively connects to the drive assembly and is movable relative to the housing to actuate the drive assembly to move the jaw members.

A switch is disposed on the housing and is activatable to selectively deliver energy of a first electrical potential to at least one jaw member for treating tissue. First and second toggle links are included which operatively connect each one of the pair of handles to the drive assembly. Each of the toggle links includes first and second anchoring elements, the first anchoring element operatively engaging the handle and the second anchoring element operatively engaging the drive assembly.

In one embodiment, the first and second anchoring elements each include a pair of tapered double tangs which operatively engage the handle and the drive assembly, respectively, in a snap-fit manner. Each pair of double tangs may include a step at a proximal end thereof for seating each pair of double tangs within a respective aperture defined within the handle and the drive assembly.

A slot may be defined between each pair double tangs. The slots may be oriented such that the greatest cross sectional area of the double tangs offsets an applied load on the forceps thereby preventing failure of the toggle links during actuation of the handles.

BRIEF DESCRIPTION OF THE DRAWINGS

Various embodiments of the subject instrument are described herein with reference to the drawings wherein:

FIG. 1A is a top, perspective view of an endoscopic forceps shown in an open configuration and including a housing, a handle assembly, a shaft and an end effector assembly according to the present disclosure;

FIG. 1B is a top, perspective view of the endoscopic forceps of FIG. 1A showing the end effector assembly in a closed configuration according to the present disclosure;

FIG. 2 is a bottom, perspective view of the endoscopic forceps of FIG. 1A;

FIG. 3A is an enlarged left, perspective view of the end effector assembly of FIG. 1A;

FIG. 3B is an enlarged left, perspective view of the end effector assembly of FIG. 1B;

FIG. 3C is an enlarged side view of the end effector assembly of FIG. 1A;

FIG. 3D is an enlarged end view of the end effector assembly of FIG. 1A;

FIG. 4 is a top, internal perspective view of the forceps of FIG. 1A shown without a housing cover;

FIG. 5A is an enlarged, top view of the forceps of FIG. 1A showing the disposition of the internal components when the forceps is in an open configuration;

FIG. 5B is an enlarged, top view of the forceps of FIG. 1B showing the disposition of the internal components when the forceps is in a closed configuration;

FIG. 6A is an enlarged perspective view of the internal working components of the forceps of FIG. 1B showing a knife actuator in an un-actuated position;

FIG. 6B is an enlarged perspective view of the internal working components of the forceps of FIG. 1 B showing a knife actuator being actuated;

FIG. 7 is an enlarged side view of the knife actuator in an un-actuated position;

FIG. 8A is a greatly-enlarged, top cross sectional view of an end effector of the end effector assembly showing a knife of the knife actuator in a proximal-most or unactuated position;

FIG. 8B is a greatly-enlarged, top cross sectional view of the end effector assembly of FIG. 8A showing the position of the knife after actuation;

FIG. 9A is an enlarged, top view showing the handle assembly in an unactuated position;

FIG. 9B is an enlarged, top view showing the handle assembly after actuation;

FIG. 10A is a greatly-enlarged, side cross sectional view of the end effector assembly shown in an open configuration;

FIG. 10B is a greatly-enlarged, side cross sectional view of the end effector assembly shown in a closed configuration;

FIG. 10C is a greatly-enlarged, front perspective view of a bottom jaw member of the end effector assembly showing the knife of the knife actuator in a proximal-most or unactuated position;

FIG. 10D is a greatly-enlarged, front perspective view of the bottom jaw member of FIG. 10C showing the position of the knife after actuation;

FIG. 11A is an enlarged, top view similar to FIG. 9B showing the knife actuator after actuation;

FIG. 11B is a greatly-enlarged, side cross sectional view of the end effector assembly showing the position of the knife after actuation;

FIG. 12 is top, perspective view of the forceps of FIG. 1B showing rotation of the end effector assembly;

FIG. 13 is a top, perspective view of the forceps with parts separated;

FIG. 14 is an enlarged, perspective view of the housing with parts separated;

FIG. 15A is a greatly-enlarged, perspective view of the bottom jaw of the end effector assembly with parts separated;

FIG. 15B is a greatly-enlarged, perspective view of the top jaw of the end effector assembly with parts separated;

FIG. 16 is an enlarged, perspective view of a circuit board for use with the forceps according to the present disclosure;

FIG. 17 is a greatly-enlarged, perspective view of the elongated shaft for housing various moving parts of the drive assembly and knife assembly;

FIG. 18 is a top, perspective view of an alternate safety lockout mechanism for use with the forceps of FIG. 1A;

FIG. 19 is a top view of a flex circuit board for use with the forceps of FIG. 1A;

FIG. 20 is a schematic diagram showing the operational features of a safety switch of the flex circuit board of FIG. 19;

FIG. 21 is an internal perspective view showing the assembly of the safety switch of FIG. 19 in the housing of the forceps;

FIG. 22A-22C are internal views showing the operational movements of the safety lockout mechanism of FIG. 18 as the lockout mechanism engages the safety switch of the flex circuit board;

FIG. 23 is a schematic electrical diagram of the electrical switching assembly;

FIG. 24 is a computer simulation showing the movement of the an intensity control on the switching assembly;

FIG. 25 is an enlarged view of the intensity control actuator;

FIG. 26 is a computer-simulated, enlarged internal view of the intensity control actuator mechanically engaged within a detent track disposed in the housing;

FIG. 27 is a computer-simulated, enlarged internal top view of the intensity control actuator mechanically engaged atop a railway defined in the housing;

FIG. 28 is a computer-simulated perspective view showing a tapered toggle link operatively connecting the drive assembly to a handle of the handle assembly;

FIG. 29 is an enlarged, perspective view of one embodiment of a toggle link showing a pair double tang anchoring element; and

FIG. 30 is an enlarged top view showing the orientation of a pair of slots each defined between one of the pair double tang anchoring elements.

DETAILED DESCRIPTION

Turning now to FIGS. 1A-2, one embodiment of a combination endoscopic bipolar and monopolar forceps 10 is shown for use with various surgical procedures and generally includes a housing 20, a handle assembly 30, a rotating assembly 80, a knife trigger assembly 70 and an end effector assembly 100 which mutually cooperate to grasp, seal and divide tubular vessels and vascular tissue (FIGS. 10A and 10B). Although the majority of the figure drawings depict a forceps 10 for use in connection with endoscopic surgical procedures, the present disclosure may be used for more traditional open surgical procedures. For the purposes herein, the forceps 10 is described in terms of an endoscopic instrument; however, it is contemplated that an open version of the forceps may also include the same or similar operating components and features as described below.

Forceps 10 includes a shaft 12 which has a distal end 16 dimensioned to mechanically engage the end effector assembly 100 and a proximal end 14 which mechanically engages the housing 20. Details of how the shaft 12 connects to the end effector are described in more detail below. The proximal end 14 of shaft 12 is received within the housing 20 and the connections relating thereto are also described in detail below. In the drawings and in the descriptions which follow, the term “proximal”, as is traditional, will refer to the end of the forceps 10 which is closer to the user, while the term “distal” will refer to the end which is further from the user.

Forceps 10 also includes an electrosurgical cable 310 which connects the forceps 10 to a source of electrosurgical energy, e.g., a generator 500 (See FIG. 16). Generators such as those sold by Valleylab—a division of Tyco Healthcare LP, located in Boulder Colo. may be used as a source of both bipolar electrosurgical energy for sealing vessel and vascular tissues as well as monopolar electrosurgical energy which is typically employed to coagulate or cauterize tissue. It is envisioned that the generator 500 may include various safety and performance features including isolated output, impedance control and/or independent activation of accessories. The electrosurgical generator 500 may also be configured to include Valleylab's Instant Response™ technology which provides an advanced feedback system to sense changes in tissue two-hundred (200) times per second and adjust voltage and current to maintain appropriate power. The Instant Response™ technology is believed to provide one or more of the following benefits to surgical procedure:

-   -   Consistent clinical effect through all tissue types;     -   Reduced thermal spread and risk of collateral tissue damage;     -   Less need to “turn up the generator”; and     -   Designed for the minimally invasive environment.

As best show in FIG. 16, cable 310 is divided into cable leads 310 a and 310 b which are configured to connect the forceps to the electrosurgical generator 500 by virtue of one. or more connectors or by virtue of separate so-called “flying leads” which are configured to connect to the generator 500 at a single location and provide either bipolar, monopolar (or a combination thereof) energy as desired or based upon the particular instrument configuration set up by the surgeon prior to surgery. One example of a universal electrical connector is being currently developed by Valleylab, Inc. of Boulder, Colo. a division of Tyco Healthcare, LP and is the subject of U.S. patent application Ser. No. 10/718,114 entitled “CONNECTOR SYSTEMS FOR ELECTROSURGICAL GENERATOR” the entire contents of which is incorporated by reference herein.

Handle assembly 30 includes two movable handles 30 a and 30 b disposed on opposite sides of housing 20. Handles 30 a and 30 b are movable relative to one another to actuate the end effector assembly 100 as explained in more detail below with respect to the operation of the forceps 10.

As best seen in the exploded view of FIG. 13, housing 20 is formed from two (2) housing halves 20 a and 20 b which each include a plurality of interfaces 205 which are dimensioned to mechanically align and engage one another to form housing 20 and enclose the internal working components of forceps 10. It is envisioned that a plurality of additional interfaces (not shown) may disposed at various points around the periphery of housing halves 20 a and 20 b for ultrasonic welding purposes, e.g., energy direction/deflection points. It is also contemplated that housing halves 20 a and 20 b (as well as the other components described below) may be assembled together in any fashion known in the art. For example, alignment pins, snap-like interfaces, tongue and groove interfaces, locking tabs, adhesive ports, etc. may all be utilized either alone or in combination for assembly purposes.

Rotating assembly 80 is mechanically coupled to housing 20 and is rotatable approximately 90 degrees in either direction about a longitudinal axis “A” (See FIGS. 1A-2 and 12). Details of the rotating assembly 80 are described in more detail with respect to FIGS. 12-14. Rotating assembly 80 includes two halves 81 a and 81 b which, when assembled, form the rotating assembly 80 which, in turn, supports the elongated shaft 12 which houses drive assembly 60 and the knife assembly 70. Halves 81 a and 81 b are mechanically engaged to housing 20 atop flanges 82 a and 82 b, respectively, during assembly and may include other mechanical interfaces dimensioned to securely engage the two halves 81 a and 81 b of the rotating assembly 80, e.g., alignment pins, snap-fit interfaces, ultrasonic welding points, etc.

As mentioned above, end effector assembly 100 is attached at the distal end 16 of shaft 12 and includes a pair of opposing jaw members 110 and 120 (See FIGS. 3A-3D). Handles 30 a and 30 b of handle assembly 30 ultimately connect to drive assembly 60 which, together, mechanically cooperate to impart movement of the jaw members 110 and 120 from an open position wherein the jaw members 110 and 120 are disposed in spaced relation relative to one another, to a clamping or closed position wherein the jaw members 110 and 120 cooperate to grasp tissue (FIGS. 10A and 10B) therebetween.

It is envisioned that the forceps 10 may be designed such that it is fully or partially disposable depending upon a particular purpose or to achieve a particular result. For example, end effector assembly 100 may be selectively and releasably engageable with the distal end 16 of the shaft 12 and/or the proximal end 14 of shaft 12 may be selectively and releasably engageable with the housing 20 and the handle assembly 30. In either of these two instances, the forceps 10 would be considered “partially disposable” or “reposable”, i.e., a new or different end effector assembly 100 (or end effector assembly 100 and shaft 12) selectively replaces the old end effector assembly 100 as needed. As can be appreciated, the presently disclosed electrical connections may have to be altered to modify the instrument to a reposable forceps.

Turning now to the more detailed features of the present disclosure as described with respect to FIGS. 1A-16, handles 30 a and 30 b each include an aperture 33 a and 33 b, respectively, defined therein which enables a user to grasp and move each respective handle 30 a and 30 b relative to one another. Handles 30 a and 30 b also include ergonomically-enhanced gripping elements 39 a and 39 b, respectively, disposed along an outer edge thereof which are designed to facilitate gripping of the handles 30 a and 30 b during activation. It is envisioned that gripping elements 39 a and 39 b may include one or more protuberances, scallops and/or ribs to enhance gripping.

As best illustrated in FIGS. 1A and 7, handles 30 a and 30 b are configured to extend outwardly on opposite sides from a transverse axis “B” defined through housing 20 which is perpendicular to longitudinal axis “A”. Handles 30 a and 30 b are movable relative to one another in a direction parallel to axis “B” to open and close the jaw members 110 and 120 as needed during surgery. This forceps style is commonly referred to as an “in-line” or hemostat style forceps as compared to a so-called “pistol grip” style forceps or endoscopic instrument. In-line hemostats or forceps are more commonly manufactured for open surgical procedures and typically include a pair of shafts having integrally coupled handles which are movable relative to one another to open and close the jaw members disposed at the distal end thereof.

As best illustrated in FIG. 5A and as mentioned above, handles 30 a and 30 b mechanically couple to the housing 20 and are movable relative to the housing (and each other) to affect movement of the jaw members 110 and 120 from the open or spaced configuration to a closed position about tissue. Each handle, e.g., handle 30 a shown in FIG. 7, is also configured to extend downwardly at an angle alpha (a) relative to the longitudinal axis “A”. It is envisioned that manufacturing the handles 30 a and 30 b to extend in this fashion facilitates and enhances gripping and manipulation of the forceps 10 during operating conditions. It is envisioned that the angle (a) of the handles 30 a and 30 b of forceps 10 may be adjustable to allow different users to essentially “customize” the handles 30 a and 30 b for a particular use of for a particular hand size. Alternatively, different forceps 10 may be manufactured with different pre-fixed angles (α) for use with specific surgical procedures, for particular hand sizes (i.e., small, medium and large) and/or for other surgical purposes. It is further contemplated that in a particularly useful embodiment, the angle (α) of the handle ranges from about zero degrees (0°) degrees to about thirty-five degrees (35°).

As best seen in FIGS. 5A, 5B, 13 and 14, the distal end 34 and 37 of each handle 30 a and 30 b, respectively, is selectively moveable about pivot pins 34 a and 34 b attached to a distal end 21 of the housing 20. As explained in more detail below, movement of the handles relative to one another imparts movement of the jaw members 110 and 120 relative to one another. The distal ends 34 and 37 are configured to include complimentary gear teeth 34 a′ and 34 b′ which are configured to intermesh with one another to facilitate consistent movement of the handle members 30 a and 30 b relative to one another and to enhance actuation of the jaw members 110 and 120.

In FIG. 14, the proximal end 30 a′ and 30 b′ of the each handle 30 a and 30 b, respectively, includes a flange 31 a and 31 b which extends from the proximal end 30 a′ and 30 b′ of each handle 30 a and 30 b towards the housing 20. Each of the flanges 31 a and 31 b includes an aperture 36 c′ and 36 d′ disposed therein for receiving an end 36 c and 36 d of a toggle link 35 a and 35 b, respectively. The opposite ends 36 a and 36 b of the toggle links 35 a and 35 b are configured to attached to an actuating or drive collar 69 of the drive assembly 60 through corresponding apertures 36 a′ and 36 b′ defined therethrough. It is envisioned that the toggle links 35 a and 35 b may be dimensioned in a generally S-shaped configuration to attach the handles 30 a and 30 b to the drive collar 69 or the toggle links 35 a and 35 b may be generally U-shaped (as disclosed) to accomplish this purpose. It is contemplated that dimensioning the toggle links 35 a and 35 b in a U-shaped configuration may reduce buckling during actuation.

In one envisioned embodiment, the toggle links, e.g., toggle link 35 a′, are generally symmetrical and include snap-like mechanical interfaces at the distal ends thereof to facilitate manufacture and assembly. More particularly and as best shown in FIGS. 28-30, link 35 a′ includes two double tang anchoring elements 36 d″ and 36 b″ at opposite ends thereof which are designed to correspondingly engage the drive collar 69 to a respective handle, e.g., 30 b. In other words, anchor element 36 d″ is configured to engage aperture 36 d′ of the handle 30 b and anchor element 36 b″ is configured to engage aperture 36 b′ of drive collar 69 to link the drive collar 69 to handle 30 b.

As can be appreciated, the geometry of each respective double tang anchor elements 36 b″ and 36 d″ includes a pair of tapered double tangs 37 a, 37 b and 37 c, 37 d. Each pair of double tangs 37 a, 37 b and 37 c, 37 d, respectively, includes a step 39 a′, 39 b′ and 39 c′ and 39 d′, respectively, at a proximal end thereof. Each pair of opposing tangs 37 a, 37 b and 37 c, 37 d includes a slot 38 a and 38 b, respectively, defined therebetween to allow each tang 37 a, 37 b and 37 c, 37 d to deflect inwardly to reduce the cross section of the anchoring element 36 d″ and 36 b″. As can be appreciated, upon assembly into a corresponding aperture, e.g., 36 d and 36 b, the taper of each tang 37 a, 37 b and 37 c, 37 d forces each tang 37 a, 37 b and 37 c, 37 d inwardly to reduce the cross section of each anchoring element 36 d″ and 36 b″ to facilitate engagement of the anchoring elements 36 d″ and 36 b″ within a corresponding aperture 36 d′ and 36 b′. Once the double tangs 37 a, 37 b and 37 c, 37 d are engaged within the respective apertures 36 d″ and 36 b″ past steps 39 a′, 39 b′ and 39 c′ and 39 d′, the tangs 37 a, 37 b and 37 c, 37 d spring outwardly to engage and seat the respective anchoring element 36 d″ and 36 b″ within the corresponding apertures 36 d′ and 36 b′. Once assembled, the slots 38 a and 38 b are preferably oriented such that the greatest cross sectional area of each anchoring element 36 d″ and 36 b″, i.e., the area with the most material, resides in the direction of the load when applied to close the jaw members 110 and 120 (See FIGS. 28 and 30). This prevent the toggle links35 a′ and 35 b′ from failing due to an overstressed condition or repeated use.

As can be appreciated, movement of the handles 30 a and 30 b from an open or spaced apart configuration to a closed position towards the housing forces the actuating collar 69 proximally against a spring 63 which, in turn, translates a drive shaft 17 proximally to close the jaw members 110 and 120 (see FIGS. 7-9). The operative relationship of the drive collar 69 and the handle assembly 30 is explained in detail below with respect to the operation of the forceps 10.

The handles 30 a and 30 b force the toggle links 35 a and 35 b to rotate along the longitudinal axis “A” beyond a parallel orientation with shaft 17 or longitudinal axis “A” such that, upon release, the force of spring 63 maintains the toggle links 35 a and 35 b in an over center or an over-extended (or past parallel) configuration thereby locking the handles 30 a and 30 b (and therefore the jaw members 110 and 120) relative to one another (FIG. 9B). Movement of the handles 30 a and 30 b away from one another (and the housing 20) unlocks and opens the handles 30 a and 30 b and, in turn, the jaw members 110 and 120 for subsequent grasping or re-grasping of tissue. In one embodiment, the handles 30 a and 30 b may be biased in an open configuration to facilitate handling and manipulation of the forceps within an operative field. Various spring-like mechanisms are contemplated which may be utilized to accomplish this purpose.

Handle 30 a also includes a locking flange 32 which is disposed between the distal and proximal ends 34 a′ and 30 a′, respectively, which extends towards the housing 20 and moves relative thereto when handle 30 a is actuated. Locking flange 32 includes a lockout element 32′ (FIG. 14) which is dimensioned to prevent actuation of the knife assembly 70 when handle 30 a is disposed in a spaced-apart or open configuration. Actuation or movement of the handle 30 a towards the housing 20 disengages the lockout element 32 to allow movement of the knife assembly 70 (e.g., collar 74) to separate tissue as explained in more detail below.

Movable handles 30 a and 30 b are designed to provide a distinct lever-like mechanical advantage over conventional handle assemblies due to the unique position of the toggle links 35 a and 35 b which, when actuated, rotate along the longitudinal axis “A” to displace the actuation or drive collar 69. In other words, it is envisioned that enhanced mechanical advantage for actuating the jaw members 110 and 120 is gained by virtue of the unique position and combination of several inter-cooperating elements (i.e., opposing handles 30 a, 30 b, toggle links 35 a, 35 b and gear teeth located at the distal ends 34 and 37 of the handle members 30 a, 30 b, respectively) which reduce the overall user forces necessary to obtain and maintain the jaw members 110 and 120 under ideal operating pressures of about 3 kg/cm² to about 16 kg/cm². In other words, it is envisioned that the combination of these elements and their positions relative to one another enables the user to gain lever-like mechanical advantage to actuate the jaw members 110 and 120 enabling the user to close the jaw members 110 and 120 with lesser force while still generating the required forces necessary to effect a proper and effective tissue seal. The details relating to the various movements of the above-identified elements are explained below with respect to the operation of the forceps 10.

As shown best in FIGS. 3A-3D, 10A-10D and 15A-15D, the end effector assembly 100 includes opposing jaw members 110 and 120 which cooperate to effectively grasp tissue for sealing purposes. The end effector assembly 100 is designed as a bilateral assembly, i.e., both jaw members 110 and 120 pivot relative to one another about a pivot pin 185 disposed therethrough.

A reciprocating drive sleeve 17 (See FIG. 17) is slidingly disposed within the shaft 12 and is remotely operable by the drive assembly 60 as explained in more detail below. Drive sleeve 17 includes a bifurcated distal end composed of halves 17 a and 17 b, respectively, which define a cavity 17′ therebetween for receiving jaw members 110 and 120. More particularly and as best illustrated in FIGS. 15A and 15B, jaw members 110 and 120 include proximal flanges 113 and 123 (See FIGS. 15A and 15B), respectively, which each include an elongated angled slot 181 a and 181 b, respectively, defined therethrough. A drive pin 180 (See FIGS. 10A and 10B) mounts jaw members 110 and 120 to the end of a rotating shaft 18 and within cavity 17′ disposed at the distal ends 17 a and 17 b of drive sleeve 17.

Upon actuation of the drive assembly 60, the drive sleeve 17 reciprocates which, in turn, causes the drive pin 180 to ride within slots 181 a and 181 b to open and close the jaw members 110 and 120 as desired. The jaw members 110 and 120, in turn, pivot about pivot pin 185 disposed through respective pivot holes 186 a and 186 b disposed within flanges 113 and 123. As can be appreciated, squeezing handles 30 a and 30 b toward the housing 20 pulls drive sleeve 17 and drive pin 180 proximally to close the jaw members 110 and 120 about tissue 420 grasped therebetween and pushing the sleeve 17 distally opens the jaw members 110 and 120 for grasping purposes.

As best shown in FIG. 15B, jaw member 110 also includes a support base 119 which extends distally from flange 113 and which is dimensioned to support an insulative plate 119′ thereon. Insulative plate 119′, in turn, is configured to support an electrically conductive tissue engaging surface or sealing plate 112 thereon. It is contemplated that the sealing plate 112 may be affixed atop the insulative plate 119′ and support base 119 in any known manner in the art, snap-fit, over-molding, stamping, ultrasonically welded, etc. Support base 119 together with the insulative plate 119′ and electrically conductive tissue engaging surface 112 are encapsulated by an outer insulative housing 114. Outer housing 114 includes a cavity 114 a which is dimensioned to securely engage the electrically conductive sealing surface 112 as well as the support base 119 and insulative plate 119′. This may be accomplished by stamping, by overmolding, by overmolding a stamped electrically conductive sealing plate and/or by overmolding a metal injection molded seal plate. All of these manufacturing techniques produce jaw member 110 having an electrically conductive surface 112 which is substantially surrounded by an insulating substrate 114.

For example and as shown in FIG. 15B, the electrically conductive sealing plate 112 includes a mating portion 112 a which surrounds the periphery of the sealing plate 112. Flange 112 a is designed to matingly engage an inner lip 117 of the outer insulator 114. It is envisioned that lead 325 a extending from circuit board 170 or generator 500 (See FIG. 16) terminates within the outer insulator 114 and is designed to electro-mechanically couple to the sealing plate 112 by virtue of a crimp-like connection 326 a. For example, the insulator 119′, electrically conductive sealing surface 112 and the outer, non-conductive jaw housing 114 are preferably dimensioned to limit and/or reduce many of the known undesirable effects related to tissue sealing, e.g., flashover, thermal spread and stray current dissipation.

It is envisioned that the electrically conductive sealing surface 112 may also include an outer peripheral edge which has a pre-defined radius and the outer housing 114 meets the electrically conductive sealing surface 112 along an adjoining edge of the sealing surface 112 in a generally tangential position. At the interface, the electrically conductive surface 112 is raised relative to the outer housing 114. These and other envisioned embodiments are discussed in co-pending, commonly assigned Application Serial No. PCT/US01/11412 entitled “ELECTROSURGICAL INSTRUMENT WHICH REDUCES COLLATERAL DAMAGE TO ADJACENT TISSUE” by Johnson et al. and co-pending, commonly assigned Application Serial No. PCT/US01/11411 entitled “ELECTROSURGICAL INSTRUMENT WHICH IS DESIGNED TO REDUCE THE INCIDENCE OF FLASHOVER” by Johnson et al., the entire contents of both of which being hereby incorporated by reference herein.

The electrically conductive surface or sealing plate 112 and the outer housing 114, when assembled, form a longitudinally-oriented slot 115 a defined therethrough for reciprocation of the knife blade 190. It is envisioned that the knife channel 115 a cooperates with a corresponding knife channel 115 b defined in jaw member 120 to facilitate longitudinal extension of the knife blade 190 along a preferred cutting plane to effectively and accurately separate the tissue along the formed tissue seal. As best illustrated in FIGS. 8A, 8B, 15A and 15B, knife channel 115 runs through the center of the jaw members 110 and 120, respectively, such that a blade 190 from the knife assembly 70 can cut the tissue grasped between the jaw members 110 and 120 when the jaw members 110 and 120 are in a closed position. More particularly and as mentioned above with respect to the discussion of the handle assembly 30, handle 30 a includes a lockout flange which prevents actuation of the knife assembly 70 when the handle 30 a is open thus preventing accidental or premature activation of the blade 190 through the tissue.

As explained above and as illustrated in FIGS. 15A and 15B, the knife channel 115 is formed when the jaw members 110 and 120 are closed. In other words, the knife channel 115 includes two knife channel halves—knife channel half 115 a disposed in sealing plate 112 of jaw member 110 and knife channel half 115 b disposed sealing plate 122 of jaw member 120. It is envisioned that the knife channel 115 may be configured as a straight slot with no degree of curvature which, in turn, causes the knife 190 to move through the tissue in a substantially straight fashion. Alternatively, the knife channel 115 may be dimensioned to include some degree of curvature to cause the knife 190 to move through tissue in a curved fashion. Insulating plate 119′ also forms part of the knife channel 115 and includes a channel 115 a′ defined therein which extends along insulating plate 119′ and which aligns in vertical registration with knife channel half 115 a to facilitate translation of distal end 192 of the knife 190 therethrough.

The electrically conductive sealing plate 112 of jaw member 110 also includes a monopolar extension 112 a which allows a surgeon to selectively coagulate tissue when disposed in a monopolar activation mode as explained in more detail below with respect to the operation of the forceps 10. Monopolar extension 112 a is preferably integrally associated with conductive sealing plate 112 but may also be selectively extendible depending upon a particular purpose. The shape and dimension of the monopolar extension 112 a may be dimensioned to match the overall contour of the curving contour of the jaw member 110 or the jaw housing 114. The edges of the monopolar extension 112 a may be dimensioned to include radii specifically dimensioned to reduce current density along the edges thereof, e.g., smooth curves and transition points. The thickness of the monopolar extension 112 a is preferably within a range of about 0.010 inches +/−0.005 inches. The width of the monopolar extension 112 a is preferably about 0.084 inches +/−0.010 inches to permit the creation of an enterotomy that the jaw member(s) may pass therethrough for the purposes of mechanically spreading tissue. The length is preferably about 0.040 inches +/−0.010 inches. Commonly-owned U.S. application Ser. No. 10/970,307 entitled “BIPOLAR FORCEPS HAVING MONOPOLAR EXTENSION” and U.S. application Ser. No. 10/988,950 entitled “BIPOLAR FORCEPS HAVING MONOPOLAR EXTENSION” disclose various embodiments of a monopolar extension which may be configured for use with forceps 10 of the present disclosure. The entire contents of both of these applications are hereby incorporated by reference herein.

Jaw member 120 includes similar elements to jaw member 110 such as jaw housing 124 which encapsulates a support plate 129, an insulator plate 129′ and an electrically conductive sealing surface 122. Likewise, the electrically conductive surface 122 and the insulator plate 129′, when assembled, include respective longitudinally-oriented knife channels 115 a and 115 a′ defined therethrough for reciprocation of the knife blade 190. As mentioned above, when the jaw members 110 and 120 are closed about tissue, knife channels 115 a and 11 5 b form a complete knife channel 115 to allow longitudinal extension of the knife 190 in a distal fashion to sever tissue along a tissue seal. It is also envisioned that the knife channel 115 may be completely disposed in one of the two jaw members, e.g., jaw member 120, depending upon a particular purpose. It is also envisioned that jaw member 120 may be assembled in a similar manner as described above with respect to jaw member 110.

As best seen in FIG. 15A, jaw member 120 includes a series of stop members 90 disposed on the inner facing surface of the electrically conductive sealing surface 122 to facilitate gripping and manipulation of tissue and to define a gap “G” (FIG. 10B) between opposing jaw members 110 and 120 during sealing and cutting of tissue. It is envisioned that the series of stop members 90 may be employed on one or both jaw members 110 and 120 depending upon a particular purpose or to achieve a desired result. A detailed discussion of these and other envisioned stop members 90 as well as various manufacturing and assembling processes for attaching and/or affixing the stop members 90 to the electrically conductive sealing surfaces 112, 122 are described in commonly-assigned, co-pending U.S. Application Serial No. PCT/US01/11413 entitled “VESSEL SEALER AND DIVIDER WITH NON-CONDUCTIVE STOP MEMBERS” by Dycus et al. which is hereby incorporated by reference in its entirety herein.

Jaw member 120 is connected to a second electrical lead 325 b extending from circuit board 170 or generator 500 (See FIG. 16) which terminates within the outer insulator 124 and is designed to electro-mechanically couple to the sealing plate 122 by virtue of a crimp-like connection 326 b. As explained in more detail below, leads 325 a and 325 b allow a user to selectively supply either bipolar or monopolar electrosurgical energy to the jaw members 110 and 120 as needed during surgery.

Jaw members 110 and 120 are electrically isolated from one another such that electrosurgical energy can be effectively transferred through the tissue to form a tissue seal. For example and as best illustrated in FIGS. 15A and 15B, each jaw member, e.g., 110, includes a uniquely-designed electrosurgical cable path disposed therethrough which transmits electrosurgical energy to the electrically conductive sealing surface 112. Cable lead 325 a is held loosely but securely along the cable path to permit rotation of the jaw members 110 and 120. As can be appreciated, this isolates electrically conductive sealing surface 112 from the remaining operative components of the end effector assembly 100, jaw member 120 and shaft 12. The two electrical potentials are isolated from one another by virtue of the insulative sheathing surrounding the cable leads 325 a and 325 b.

As mentioned above, jaw members 110 and 120 are engaged to the end of rotating shaft 18 by pivot pin 185 such that rotation the rotating assembly 80 correspondingly rotates shaft 18 (along with sleeve 17 and knife drive rod 71) which, in turn, rotates end effector assembly 100 (See FIG. 12). More particularly, the distal end of rotating shaft 18 is bifurcated to include ends 18 a and 18 b which define a channel therein for receiving jaw members 110 and 120. Pivot pin 185 secures the jaw members 110 and 120 to ends 18 a and 18 b through aperture 186 a and 186 b defined through jaw members 110 and 120, respectively. As best seen in FIGS. 13 and 17, rotating shaft 18 is dimensioned to slidingly receive knife drive rod 71, knife 190 and a knife guide 197 therein. Rotating shaft 18, in turn, is rotatingly received within drive sleeve 17 which as mentioned above connects to the drive assembly 60. The details with respect to the knife assembly are explained in more detail with respect to FIGS. 5A, 5B, 6A, 6B, 7, 8A and 8B.

Rotating shaft 18 and drive shaft 17 are fixed to the rotating assembly 80 by two rotating tabs which are engaged through slot 18 c in the rotating shaft 18 such that rotating of the rotating member correspondingly rotates the rotating shaft 18. It is envisioned that the drive shaft and the rotating shaft may be affixed to the rotating assembly in other ways known in the art, snap-fit, friction fit, etc.

FIGS. 13 and 14 show the details of the forceps 10 and the component features thereof, namely, the housing 20, the drive assembly 60, the rotating assembly 80, the knife assembly 70 and the handle assembly 30. More particularly, FIG. 13 shows the entire forceps 10 along with the above-identified assemblies and components thereof in an exploded condition and FIG. 14 shows an exploded view of the housing 20 and the components contained therein.

Housing 20 includes housing halves 20 a and 20 b which, when mated, form housing 20. As can be appreciated, housing 20, once formed, forms an internal cavity 25 which houses the various assemblies identified above which will enable a user to selectively manipulate, grasp, seal and sever tissue in a simple, effective, and efficient manner. Each half of the housing, e.g., half 20 b, includes a series of mechanical interfacing components, e.g., 205 which align and/or mate with a corresponding series of mechanical interfaces (not shown) to align the two housing halves 20 a and 20 b about the inner components and assemblies. The housing halves 20 a and 20 b may then be sonic welded or otherwise matingly engaged to secure the housing halves 20 a and 20 b once assembled.

As mentioned above, the handle assembly 30 includes two movable handles 30 a and 30 b which each cooperate with a toggle link 35 a and 35 b, respectively, to actuate the actuating or drive collar 69 of the drive assembly 60. The drive collar, in turn, reciprocates drive sleeve 17 to open and close the jaw members 110 and 120 as described above. Movable handles 30 a and 30 b are designed to provide a distinct lever-like mechanical advantage over conventional handle assemblies due to the unique position of the toggle links 35 a and 35 b which, when actuated, rotate along the longitudinal axis “A” to displace the actuation collar 69. More particularly and as mentioned above, it is envisioned that enhanced lever-like mechanical advantage for actuating the jaw members 110 and 120 is gained by virtue of the unique position and combination of various inter-cooperating elements such as the toggle links 35 a and 35 b and the gear teeth 34 a and 34 b at the distal end of the handles 30 a and 30 b which cooperate to reduce the overall user forces necessary to obtain and maintain the jaw members under ideal operating pressures of about 3 kg/cm² to about 16 kg/cm².

As mentioned above, movement of the handles 30 a and 30 b from an open or spaced apart configuration to a closed position towards the housing 20 forces the actuating collar 69 proximally against spring 63 which, in turn, translates drive sleeve 17 proximally to close the jaw members 110 and 120. Moreover, as the handles 30 a and 30 b rotate to a closed position, the handles 30 a and 30 b force the toggle links 35 a and 35 b to rotate along the longitudinal axis “A” beyond a parallel orientation with longitudinal axis “A” such that upon release of the handles 30 a and 30 b from a closed position, the force of spring 63 maintains the toggle links 35 a and 35 b in an over-extended\over-centered (i.e., past parallel) configuration thereby locking the handles 30 a and 30 b (and therefore the jaw members 110 and 120) relative to one another (See FIGS. 9A and 9B). To unlock the jaw members 110 and 120, the handles 30 a and 30 b are moved away from one another (and the housing 20) to return the toggle links 35 a and 35 b to at least a parallel orientation with respect to longitudinal axis “A” which unlocks and opens the handles 30 a and 30 b and, in turn, the jaw members 110 and 120 for subsequent grasping or re-grasping of tissue. Once the handles 30 a and 30 b are opened past parallel the force of spring 63 facilitates opening of the handles 30 a and 30 b and the jaw members 110 and 120.

As mentioned above, handle 30 a also includes a locking flange 32 which is dimensioned to prevent actuation of the knife assembly 70 when handle 30 a is disposed in a spaced-apart or open configuration. Actuation or movement of the handle 30 a towards the housing 20 disengages the lockout element 32 to allow movement of the knife assembly 70 to separate tissue as explained in more detail below.

As best seen in FIG. 14, the drive assembly includes drive collar 69, spring 63 and locking sleeve 62. Toggle links 35 a and 35 b operatively connect the drive collar 69 to the handles 30 a and 30 b, respectively. The locking sleeve 62 is dimensioned to fit through an opening 67 defined through the drive collar 69 and the spring 63 is dimensioned to fit over the locking sleeve 62. The spring 63, in turn, is biased between and against the drive collar 69 and a pair of locking bolts 62 a and 62 b which to the locking sleeve 62. Upon actuation of the handles 30 a and 30 b, the toggle links 35 a and 35 b force the drive collar 69 proximally to compress the spring 63 against the locking bolts 62 a and 62 b.

As best seen in FIGS. 9A and 9B, the locking sleeve 62 and sleeve 17 are clamped or welded together at assembly. Locking sleeve 62 includes a distal collar 62′ which abuts drive collar 69 to ensure axial translation of the driving collar 69 upon actuation of the handles 30 a and 30 b. Locking sleeve 62 and sleeve 17 are also dimensioned to reciprocate through locking nuts 62 a and 62 b during actuation of handles 30 a and 30 b which enables the spring 63 to compress against locking nuts 62 a and 62 b which as mentioned above, facilitates locking the forceps 10 in a closed orientation within desired force ranges and facilitates opening of the handles 30 a and 30 b after activation of the forceps 10.

FIG. 14 also shows the rotating assembly 80 which includes two C-shaped rotating halves 81 a and 81 b which, when assembled about shaft 17, form a generally circular rotating member 81. More particularly, each rotating half, e.g., 81 b, includes a series of mechanical interfaces 83 which matingly engage a corresponding series of mechanical interfaces (not shown) in half 81 a to form rotating member 81. Half 81 b also includes a tab or protrusion (Not shown) which together with a corresponding tab or protrusion (not shown) disposed on half 81 a cooperate to matingly engage slots 17 c and 18 c on the drive shaft 17 and rotating shaft 18, respectively. As can be appreciated, this permits selective rotation of the end effector assembly 100 about axis “A” by manipulating the rotating member 80 in the direction of the arrow “R” (see FIGS. 1A and 12).

As mentioned above, the jaw members 110 and 120 may be opened, closed and rotated to manipulate tissue until sealing is desired. This enables the user to position and re-position the forceps 10 prior to activation and sealing. It is envisioned that the unique feed path of the cable leads 325 a and 325 b through the rotating assembly 80, along shaft 18 and, ultimately, to jaw members 110 and 120 enables the user to rotate the end effector assembly 100 about 170 degrees in both the clockwise and counterclockwise direction without tangling or causing undue strain on cable leads 325 a and 325 b.

As best shown in FIGS. 5A, 5B, 6A, 6B, 7, 11A, 11B and 14, the knife assembly 70 mounts atop housing 20 and is configured to selectively translate a knife bar 71 which, in turn, translates knife 190 through tissue. More particularly, the knife assembly 70 includes a finger actuator 76 having an elongated support base 72 affixed thereto which is selectively moveable parallel to longitudinal axis “A”. Elongated support base 72 includes a proximal end which is configured as a gear rack having a series of gear teeth 72 a which depend downwardly therefrom. Gear teeth 72 a are configured to mesh with a corresponding pinion gear 77 mounted for rotation on the housing 20. The pinion gear 77 also meshes with a second gear track 75 having a plurality of gear teeth 75 a disposed on a collar 74 which is slidingly translatable atop sleeve 17. As best shown in FIGS. 9A, 9B and 11A, a pin 78 attaches the collar 74 to a proximal end 71 b of knife bar 71 through slot 17 d defined through sleeve 17. Proximal translation of the finger actuator 76 in the direction “F” rotates the pinion gear 77 in a clockwise direction which, in turn, forces the second gear track 75 a distally in the direction “H” (see FIG. 7). A spring 79 biases the collar 74 against the housing 20 to automatically return the knife assembly 70 to a pre-firing position after the finger actuator 76 is released.

The knife assembly may be configure to include a mechanical fuse to prevent excessive actuation of the knife assembly. For example, pinion gear 77 may be configured to include one or more frangible or break-away elements to prevent over extension of the finger actuator in the proximal direction. As can be appreciated, configuring the pinion gear 77 in this fashion will prevent the user from overloading and damaging the delicate knife blade 190 disposed between the jaw members 110 and 120. In one embodiment, the axle of the pinion gear 77 will fracture when an excessive force of about 9 lbf or greater is applied in the direction “F” (as shown in FIG. 7). In this instance and upon fracture of the pinion axle, the spring 79 automatically returns the knife blade 190 to a retracted position to allow the separation of the jaw members 110 and 120 which allows the forceps 10 to be safely removed from the body without damaging tissue. As can be appreciated, the fracture of the pinion axle does not contaminate the surgical field and the fractured gear 77 remains within the housing 20 of the forceps 10. In addition, it is envisioned that the internal operating components of the housing 20 may be accessible in this instance to allow replacement of the pinion gear.

It is also contemplated that other elements may be configured in a similar fashion to limit overloading of the instrument and damaging delicate parts associated with the forceps 10. For example, the teeth 72 a on the rack could be dimensioned to fracture upon excessive force or the track 75 a may fracture as well. Moreover, the handles 30 a and 30 b may be equipped with a similar overloading safety mechanism which prevents over compression of the handles 30 a and 30 b and the drive assembly 60 or handle assembly 30. For example, links 35 a and 35 b may be configured to fracture upon an overloading condition or drive collar 69.

As mentioned above, the knife assembly 70 is prevented from being actuated when the jaw members 110 and 120 are opened by virtue of flange 32 disposed on handle 30 a being positioned to prevent distal activation of the collar 74 when handles 30 a and 30 b are opened. Upon movement of the handles 30 a and 30 b to a closed position, the flange 32 is positioned to allow distal translation of collar 74 to actuate the knife bar 71.

The operating features and relative movements of the internal working components of the forceps 10 are shown by phantom representation in the various figures. As the handles 30 a and 30 b are squeezed, the drive collar 69, through the mechanical advantage of the in-line toggle links 35 a and 35 b, is moved proximally which, in turn, compresses a spring 63 against the locking nuts 62 a and 62 b. As a result thereof, the drive collar 69 reciprocates locking sleeve 62 proximally which, in turn, reciprocates drive sleeve 17 proximally to closes jaw members 110 and 120. Once the jaw members 110 and 120 are closed about tissue the user can selectively energize the electrically conductive sealing plates for either monopolar activation or bipolar activation to treat tissue.

As best shown in FIGS. 6A, 14 and 16, the forceps 10 includes two switches 250 and 260 which are mounted within or atop the housing 20 and which allow a user to selectively activate the forceps 10 to selectively transmit bipolar energy to the jaw members 110 and 120 or selectively transmit monopolar energy to the jaw members 110 and 120 or to a single jaw member, e.g., jaw member 110. For the purposes herein, it is envisioned that either switch, e.g., switch 250, may be configured for monopolar activation and the other switch, e.g., switch 260, may be configured for bipolar activation. Further the switches 250 and 260 may include indicia or other identifying elements, e.g., raised protuberances, scallops, different shapes, etc., to distinguish the two switches 250 and 260 from one another which may prove especially useful during wet operating conditions.

In one particularly useful embodiment and as best shown in FIG. 6A, switches 250 and 260 are mounted within the housing 20 on opposite sides of longitudinal axis “A” and on opposite sides of the knife assembly 70. As can be appreciated, the knife assembly 70 (and actuation thereof) and the switches 250 and 260 (and the activation thereof) are conveniently located to facilitate actuation/activation by the user during operating conditions. For example, it is contemplated that the user may utilize the same finger to both activate the switches 250 and 260 to treat tissue and actuate the knife assembly 70 to cut tissue once treated.

As shown in FIGS. 6A and 16, cable 310 is fed through the housing 20 b on one side of the drive assembly 60 and electromechanically connects to a printed circuit board 172 of the switch assembly 170. More particularly, cable 310 is internally divided into a plurality of leads 311 a-311 f which are secured by a crimp-like connector 174 to a series of corresponding contacts 176 a-176 f extending from the printed circuit board 172 or to other electrically conductive leads which ultimately connect to the jaw members. Other electromechanical connections are also envisioned which are commonly known in the art, e.g., IDC connections, soldering, etc. It is envisioned the various leads 311 a-311 f are configured to transmit different electrical potentials or control signals to the printed circuit board 172 which, in conjunction with generator 500, regulates, monitors and controls the electrical energy to the jaw members 110 and 120. As mentioned above with respect to the description of the jaw members, electrical leads 325 a and 325 b extend through the rotating member 80, along shaft 18 to ultimately connect to the jaw members 110 and 120.

FIG. 23 shows a schematic representation of a control circuit 510 for use with the presently disclosed forceps 10. As mentioned above, forceps 10 is configured to operate in two independent modes of operation—bipolar mode and monopolar mode for different surgical procedures. When one of the switches 250 (S1 in FIGS. 19 and 23) or 260 (S2 in FIGS. 19 and 23) of switch assembly 170 is depressed, a contact (not shown) on the switches 250 and 260 activates the appropriate electrical potential (or potentials) to the jaw members 110 and 120 which is (are) carried through leads 325 a and/or 325 b. For example, if switch 250 (LigaSure™ activation) is depressed, the circuit board 172 signals the generator 500 to configures the forceps 10 as a bipolar forceps and lead 325 a carries a first electrical potential to jaw member 110 and lead 325 b carries a second electrical potential to jaw member 120. As such the jaw members 110 and 120 conduct bipolar energy through the tissue upon activation to create a tissue seal. FIG. 23 shows one example of contemplated electrical circuitry which may be utilized to accomplish this purpose.

If switch 260 (monopolar activation) is depressed, the circuit board 172 configures the forceps as a monopolar forceps and lead 325 a caries a first electrical potential to jaw member 110 to coagulate or otherwise treat tissue in a monopolar fashion. As mentioned above, jaw member 110 includes a monopolar extension which facilitates monopolar treatment of various tissue types, e.g., avascular tissue structures, and/or allows quick dissection of narrow tissue planes. Activation of the monopolar extension may be controlled by an activation circuit which allows the user to selectively apply monopolar energy or bipolar energy as needed during surgery. One envisioned activation circuit is disclosed in commonly-owned U.S. patent application Ser. No. 10/970,307 entitled “BIPOLAR FORCEPS HAVING MONOPOLAR EXTENSION” and U.S. application Ser. No. 10/988,950 entitled “BIPOLAR FORCEPS HAVING MONOPOLAR EXTENSION”, the entire contents of both of these applications being hereby incorporated by reference herein.

Alternatively and as best shown in FIG. 23, during the monopolar mode when switch 260 is depressed, the generator (or the printed circuit board) can direct both leads 325 a and 325 b to carry the same electrical potential to jaw members 110 and 120 depending upon a particular purpose or depending upon a desired surgical treatment, e.g., so-called “coagulative painting”. As can be appreciated, in a monopolar mode, a return pad would be necessarily placed in contact with the patient to act as a return path (not shown) for the electrical energy. The return pad in this instance would connect to the generator 500 directly or though a return pad control mechanism (not shown) which may be configured to monitor certain parameters of the return pad. Various envisioned control systems are disclosed in commonly-owned U.S. patent application Ser. No. 10/918,984 entitled “MULTIPLE RF RETURN CABLE PAD CONTACT DETECTION SYSTEM”, U.S. patent application Ser. No. 09/310,059 entitled “ELECTROSURGICAL RETURN ELECTRODE MONITOR” (now U.S. Pat. No. 6,258,085), U.S. Provisional Patent Application Ser. No. 60/616,970 entitled “DEVICE FOR DETECTING HEATING UNDER A PATIENT RETURN ELECTRODE” and U.S. Provisional Patent Application Ser. No. 60/666,798 entitled “TEMPERATURE REGULATING PATIENT RETURN ELECTRODE AND RETURN ELECTRODE MONITORING SYSTEM”, the entire contents of all of which are incorporated by reference wherein.

In a bipolar mode, the circuit 510 (schematically-illustrated in FIG. 23) electrical routes energy to the two jaw members 110 and 120. More particularly, when switch 250 is depressed an isolated circuit 520 of the circuit 510 recognizes a resistance drop thereacross which is recognized by the generator to initiate electrosurgical energy to supply a first electrical potential to jaw member 110 and a second electrical potential to jaw member 120. Switch 520 acts as an insolated control circuit and is protected by circuitry within the generator from the higher current loop which supplies electrical energy to the jaw members 110 and 120. This reduces the chances of electrical failure of the switch 260 due to high current loads during activation.

As best shown in FIG. 14, handle 30 a also includes a switch lockout mechanism 255 which may be configured to prevent activation of one or both switches 250 and 260 when the jaw members 110 and 120 are disposed in an open configuration. More particularly, lockout mechanism 255 extends from handle 30 a towards housing 20 and is selectively moveable with the handle 30 a from a first position wherein the lockout mechanism 255 prevents one or both switches 250 and 260 from being depressed to contact the circuit board 172 to a second position closer to the housing 20 wherein the lockout mechanism 255 is positioned to allow activation of switch 250 (or switches 250 and 260). It is envisioned that the lockout mechanism 255 may be configured as a purely mechanical lockout which physically prevents movement of one or both switches 250 and/or 260 or may be configured as an electromechanical lockout which includes a mechanical element which activates a safety switch to allow activation. Moreover, the switch lockout mechanism 255 may be configured such that one or both switches may be independently and exclusively activatable, i.e., only one switch may be activated at a time.

For example, flex circuit 170 may include a safety switch 171 which is activated when lockout mechanism 255 physically engages safety switch 171 to close the circuit to permit electrosurgical activation. In other words, the safety switch 171 is deflected or physically engaged (i.e., by virtue of the movement of lockout mechanism 255 when the handles 30 a and 30 b are closed) to close the electrical path and permit electrosurgical activation. Further details with respect to various embodiments of the safety switch are described below with respect to FIGS. 18-21D. It is also envisioned that a purely electrical safety switch (See FIG. 23) may be included which allows activation based upon the satisfaction of an electrical condition, e.g., optical alignment of points on the handle 30 a (or handles (30 a and 30 b), magnetic or electromagnetic alignment (or misalignment) to close a switch, proximity sensors, scanners, mercury (or the like) switches, etc. Again, the safety switch 171 may be configured such that one or both switches 250 and/or 260 may be independently and exclusively activatable, i.e., only one switch may be activated at a time.

As can be appreciated, locating the switches 250 and 260 on the housing 20 is advantageous during operating conditions since this positioning reduces the amount of electrical cable in the operating room and eliminates the possibility of activating the wrong instrument or wrong switch during a surgical procedure due to “line-of-sight” activation. An automatic safety circuit or an electromechanical or mechanical safety lock (not shown) may be employed which prevents the switches 250 and 260 from energizing the jaw members 110 and 120 in a different mode (i.e. bipolar or monopolar mode) without de-activating a safety circuit or other safety mechanism, i.e., independent and exclusive activation. For example, it may be desirable to configure the switch assembly 70 such that it must be re-set before switching between electrical modes. Re-setting may be accomplished by re-grasping tissue, re-opening the handles 30 a and 30 b, a reset switch or re-set lever, or other ways customary in the art.

As can be appreciated various switching algorithms (See FIG. 23) may be employed to activate both the bipolar mode for vessel sealing and the monopolar mode for additional tissue treatments (e.g., coagulation, dissection, etc.). It is also envisioned that the safety or lockout mentioned above may be employed as part of an algorithm to either electrically, mechanically or electromechanically “lock out” one electrical mode during activation of the other electrical mode. In addition, it is contemplated that a toggle switch (or the like) may be employed to activate one mode at a time for safety reasons.

The safety switch 171 when assembled (and when the handles 30 a′ and 30 b and jaws 110 and 120 are opened) is secured against an interior wall or ledge 173 of housing 20 b as shown in FIG. 22A. Upon movement of the handle 30 a toward housing 20 b, safety lockout 255 moves inwardly relative to the housing 20 b toward the safety switch 171 as shown in FIG. 22B. As the handles 30 a and 30 b move toward the closed position (as described in detail above), the safety lockout 255 engages the safety circuit 171′ (S3 in FIGS. 19 and 23) to complete circuit and allow selective activation of the forceps 10 (see also FIG. 23).

As best shown in FIGS. 14 and 23-27, the switching assembly may include an intensity control 150 which electromechanically connects to the circuit board 172 and which is configured to allow the user to selectively regulate the intensity of the electrosurgical energy during operating conditions. It is envisioned that the intensity control 150 is particularly configured to regulate the intensity control when the forceps is configured in a monopolar mode. In one particularly useful embodiment, intensity control 150 is elongated and includes a contact 154 which extends transversally therefrom to electro-mechanically interface with the circuit board 172 through the housing 20. An actuating knob 151 extends transversally from the opposite side of the intensity control 150 and is dimensioned to protrude from the side of housing 20 when assembled (see FIGS. 5A, 5B, 6A and 6B). In one particularly useful embodiment, intensity control 150 is configured to slide along housing 20 to regulate the intensity level as desired.

It is envisioned that the intensity control 150 may be configured to slide along the housing 20 in a discreet or continuous manner depending upon a particular purpose. For example and as best shown in FIGS. 24-27, one envisioned intensity control 150′ may be dimensioned to include an actuating knob 151′ which extends transversally from one side of the intensity control 150′ to protrude from housing 20 when assembled. A cantilevered extension 153′ having a detent 155′ at an end thereof extends generally perpendicularly to the intensity control 150′ and is centrally disposed in the intensity control 150′. The detent 155′ of the cantilevered extension 153′ is dimensioned to engage a corresponding mechanical interface or track 161′ disposed within the housing 20 (See FIG. 26). As can be appreciated mechanical advantage is created by the cantilevered extension 153′ to facilitate actuation of the detent 155′ within the housing 20.

The detent 155′ is selectively moveable (by selectively actuating the intensity knob 150′) to engage various recesses 163 a′, 163 b′, 163 c′, 163 d′ and 163 e′ disposed in the track 161′ to lock the intensity control knob 150′ at a discreet intensity setting as desired for a particular surgical purpose. It is envisioned that the track 161′ may include one or more larger recesses, e.g., recess 163 c′, to facilitate returning the intensity control 150′ to a central (as shown), proximal-most or distal-most position.

The opposing end of the intensity control 150′ opposite detent 155′ includes a slider bump or other mechanical interface 167′ which is operatively engaged atop the flexible circuit board 170 and 170′. The slide bump 167′ is configured to deflect the flexible circuit board 170 (or 170′) at varying positions as the intensity control 150′ is moved. Deflecting the circuit board 170 (or 170′) at different locations adjusts the intensity settings by controlling the impedance of the flexible printed circuit 170 or 170′ as described below. In other words, the slide bump 167′ creates enough depression force to switch the flexible circuit 170 to a different control setting. The switch occurs when one conductive layer on the flexible circuit board 170 flexes to touch another conductive layer to create an electrical connection. As can be appreciated this allows the user to selectively regulate the intensity of the electrosurgical energy during operating conditions. As shown, the forceps 10 includes five (5) different intensity settings.

As best shown in FIG. 27, the intensity control 150′ may be positioned atop a railway 169′ defined with the housing 20. The railway 169′ is configured to facilitate translational movement of the intensity control 150′ from a proximal-most position to a distal-most position atop the flexible circuit 170 (or 170′) and within the various recesses 163 a′-163 e′.

Various types of indicia 155 and/or tactile feedback elements (not shown) may be utilized to denote the position and/or intensity level of the electrical energy, e.g., numbers, graphical indicia, mechanical interfaces, etc. It is also envisioned that the user may configure the initial intensity level on the generator 500 (See FIG. 16) and the intensity control 150 on the forceps 10 may be utilized to increase or decrease the pre-set level by a certain percentage by moving knob 151.

Intensity controller 150 may be configured to function as a slide potentiometer, sliding over and along the flexible or printed circuit board (which may be configured to function as a voltage divider network or “VDN”). For example, the intensity controller 150 may be configured to have a first position wherein knob 151 is disposed at a proximal-most position (e.g., closest to the user) which corresponds to a relative low intensity setting, a second position wherein knob 151 is disposed at a distal-most position (e.g., furthest from the user) corresponding to a relative high intensity setting, and a plurality of intermediate positions wherein knob 151 is disposed at varying positions therebetween corresponding to various intermediate intensity settings. As can be appreciated, the intensity settings from the proximal end to the distal end may be reversed, e.g., high to low. One embodiment of an intensity controller 150 is disclosed in commonly-owned U.S. patent Ser. No. 11/337,990 entitled “ELECTROSURGICAL PENCIL WITH ADVANCED ES CONTROLS”, the entire contents of which being incorporated by reference herein.

As illustrated in FIG. 14 and as mentioned above, knob 151 may be dimensioned to ride along a guide channel 157 disposed within housing 20 a which is provided with a series of discreet or detented positions defining a series of positions, e.g., five, to allow easy selection of the output intensity from the low intensity setting to the high intensity setting. The series of cooperating discreet or detented positions also provide the surgeon with a degree of tactile feedback. Accordingly, in use, as intensity controller 150 slides distally and proximally, a mechanical interface 158 disposed atop contact 154 selectively engages a series of corresponding detents (not shown) to set the intensity level as well as to provide the user with tactile feedback as to when the intensity controller 150 has been set to the desired intensity setting. Alternatively, audible feedback can be produced from intensity controller 150 (e.g., a “click”), from electrosurgical energy source 500 (e.g., a “tone”) and/or from an auxiliary sound-producing device such as a buzzer (not shown).

Intensity controller 150 may also be configured and adapted to adjust the power parameters (e.g., voltage, power and/or current intensity) and/or the power verses impedance curve shape to affect the perceived output intensity. For example, the greater intensity controller 150 is displaced in a distal direction the greater the level of the power parameters transmitted to the jaw members 110 and 120 (or simply jaw member 110 when disposed in a monopolar configuration). When the forceps is disposed in a monopolar mode, current intensities can range from about 60 mA to about 240 mA with tissue having an impedance of about 2k ohms. An intensity level of 60 mA may provide very light and/or minimal cutting/dissecting/hemostatic effects. An intensity level of 240 mA provides very aggressive cutting/dissecting/hemostatic effects.

Intensity settings are typically preset and selected from a look-up table based on a desired surgical effect, surgical specialty and/or surgeon preference. The selection may be made automatically or selected manually by the user.

It is envisioned that when the forceps 10 is changed from one mode to another mode, the intensity controller 150 may be configured such that it must be reset (e.g., the knob 151 is re-positioned to the proximal-most end of guide channels 157 thus re-setting the intensity level to the preset configuration. After being reset, intensity controller 150 may be adjusted as needed to the desired and/or necessary intensity level for the mode selected.

It is envisioned and contemplated that the circuit board 172 or generator 500 may also include an algorithm which stores the last intensity level setting for each mode. In this manner, intensity controller 150 does not have to be reset to the last operative value when the particular mode is re-selected.

The present disclosure also relates to a method for treating tissue with electrosurgical energy from the electrosurgical generator 500 which includes the steps of: providing an endoscopic forceps 10 including a housing 20 having a shaft 12 affixed thereto. The shaft 12 includes first and second jaw members, 110 and 120, respectively, attached proximate a distal end of the shaft 12. An actuator or handle assembly 30 is included for moving jaw members 110 and 120 relative to one another from a first position wherein the jaw members 110 and 120 are disposed in spaced relation relative to one another to a second position wherein the jaw members 110 and 120 cooperate to grasp tissue therebetween. The switch assembly 170 is included on the housing 20 which permits the user to selectively energize the jaw members 110 and 120 in a monopolar or bipolar mode to treat tissue.

As can be appreciated and as mentioned above, the switch assembly 170 includes switches 250 and 260, printed circuit board 172 and connectors 176 a-d. An intensity control 150 may also be included with the switch assembly 170 to regulate the intensity level of the electrosurgical energy when disposed in either mode. In this particular method, the steps further include: grasping tissue between the jaw members 110 and 120; selectively activating the jaw members 110 and 120 to treat tissue disposed between the jaw members 110 and 120 in a bipolar or monopolar fashion; and selectively regulating the intensity of the electrosurgical energy by controlling the intensity control 150.

Other steps of the method may include the steps of: providing a knife assembly 70 which is configured for selective actuation of a knife and the step of selectively actuating the knife assembly 70 to advance the knife 190 to divide tissue after tissue treatment. Still other steps may include: adjusting the intensity of the electrosurgical energy as needed during operating conditions; unlocking the knife assembly 70 prior to actuation or unlocking the knife assembly 70 simultaneously when actuating the handles 30 a and 30 b from the first and second positions.

As best shown in FIG. 17, the distal end 71 a of the elongated knife bar 71 of the knife assembly 70 attaches to the knife 190 at a proximal end thereof. It is envisioned that the knife 190 may be attached to the knife bar 71 in any way known in the art, e.g., snap-fit, fiction-fit, pinned, welded, glued, etc. In the particular embodiment shown in FIG. 17, a clamp collar 197 is used to retain the knife 190 securely engaged with the knife bar 71.

Switches 250 and 260 are typically push-button-type and ergonomically dimensioned to seat within respective apertures 250′ and 260′ of housing 20 (once assembled). It is envisioned that the switches 250 and 260 permit the user to selectively activate the forceps 10 for surgical treatment of tissue. More particularly, when either switch 250 or 260 is depressed, electrosurgical energy is transferred through leads 325 a and/or 325 b to respective jaw members 110 and 120.

Again and as noted above, a safety switch 255 (or circuit or algorithm (not shown)) may be employed such that one or both of the switches 250 and 260 cannot fire unless the jaw members 110 and 120 are closed and/or unless the jaw members 110 and 120 have tissue held therebetween. In the latter instance, a sensor (not shown) may be employed to determine if tissue is grasped between jaw members. In addition, other sensor mechanisms may be employed which determine pre-surgical, concurrent surgical (i.e., during surgery) and/or post surgical conditions. These sensor mechanisms may also be utilized with a closed-loop feedback system coupled to the electrosurgical generator to regulate the electrosurgical energy based upon one or more pre-surgical, concurrent surgical or post surgical conditions. Various sensor mechanisms and feedback systems are described in commonly-owned, co-pending U.S. patent application Ser. No. 10/427,832 entitled “METHOD AND SYSTEM FOR CONTROLLING OUTPUT OF RF MEDICAL GENERATOR”, the entire contents of which being hereby incorporated by reference herein.

Turning back to FIG. 14 which shows the exploded view of the housing 20, rotating assembly 80, drive assembly 70, handle assembly 30 and switch assembly 170, it is envisioned that all of these various component parts along with the shaft 12 and the end effector assembly 100 are assembled during the manufacturing process to form a partially and/or fully disposable forceps 10. For example and as mentioned above, the shaft 12 and/or end effector assembly 100 may be disposable and, therefore, selectively/releasably engagable with the housing 20 and rotating assembly 80 to form a partially disposable forceps 10 and/or the entire forceps 10 may be disposable after use.

It is envisioned that the opposing jaw members 110 and 120 may be rotated and partially opened and closed without unlocking the knife assembly 70 which, as can be appreciated, allows the user to grip and manipulate the tissue without premature activation of the knife 190. As mentioned below, only a substantially fully closed position of the handles 30 a and 30 b will unlock the knife assembly 70 for actuation.

Once the desired position for the sealing site is determined and the jaw members 110 and 120 are properly positioned, handles 30 a and 30 b may be squeezed to actuate the drive assembly 60 to close the jaw members 110 and 120 about tissue. As mentioned above, when the handles 30 a and 30 b are fully closed about tissue the toggle links 35 a and 35 b over-rotate past parallel with the longitudinal axis “A” such that slightly releasing the handles 30 a and 30 b biases the spring 63 to lock the handles 30 a and 30 b relative to one another. As can be appreciated, when the handles 30 a and 30 b lock relative to one another, the jaw members 110 and 120, in turn, lock and secure about tissue within a pressure range of about 3 kg/cm² to about 16 kg/cm² and, preferably, with a pressure range of about 7 kg/cm² to about 13 kg/cm². The forceps 10 is now ready for selective application of electrosurgical energy and subsequent separation of the tissue (if desired).

It is envisioned that the combination of the mechanical advantage gained by the disposition of the toggle links 35 a and 35 b relative to the longitudinal axis “A” along with the mechanical advantage gained by configuring the distal ends 34 a′ and 34 b′ as inter-engaging gear teeth will facilitate and assure consistent, uniform and accurate closure pressure about the tissue within the desired working pressure range of about 3 kg/cm² to about 16 kg/cm² and, in one particularly useful embodiment, about 7 kg/cm² to about 13 kg/cm². By controlling the intensity, frequency and duration of the electrosurgical energy applied to the tissue, the user can either cauterize, coagulate/desiccate, seal and/or simply reduce or slow bleeding by activating either or both switches 250 and 260.

In one or more particularly useful embodiments, the electrically conductive sealing surfaces 112, 122 of the jaw members 110, 120, respectively, are relatively flat to avoid current concentrations at sharp edges and to avoid arcing between high points. In addition and due to the reaction force of the tissue when engaged, jaw members 110 and 120 are preferably manufactured to resist bending. For example, the jaw members 110 and 120 may be tapered along the width thereof which is advantageous since the thicker proximal portion of the jaw members 110 and 120 will resist bending due to the reaction force of the tissue.

As mentioned above, at least one jaw member, e.g., 120, may include one or more stop members 90 which limit the movement of the two opposing jaw members 110 and 120 relative to one another. The stop member(s) 90 may be dimensioned to extend from the sealing surface 122 a predetermined distance according to the specific material properties (e.g., compressive strength, thermal expansion, etc.) to yield a consistent and accurate gap distance “G” during sealing. The gap distance between opposing sealing surfaces 112 and 122 during sealing ranges from about 0.001 inches to about 0.006 inches and, in one particularly useful embodiment, between about 0.002 and about 0.003 inches. The non-conductive stop member(s) 90 may be molded onto the jaw members 110 and 120 (e.g., overmolding, injection molding, etc.), stamped onto the jaw members 110 and 120 or deposited (e.g., deposition) onto the jaw members 110 and 120. For example, one technique involves thermally spraying a ceramic material (or the like) onto the surfaces of one or both jaw members 110 and 120 to form the stop member(s) 90. Several thermal spraying techniques are contemplated which involve depositing a broad range of heat resistant and insulative materials on various surfaces to create stop members 90 for controlling the gap distance between electrically conductive surfaces 112 and 122.

As energy is being selectively transferred to the end effector assembly 100, across the jaw members 110 and 120 and through the tissue, a tissue seal forms isolating two tissue halves. At this point and with other known vessel sealing instruments, the user must remove and replace the forceps 10 with a cutting instrument (not shown) to divide the tissue halves along the tissue seal. As can be appreciated, this is both time consuming and tedious and may result in inaccurate tissue division across the tissue seal due to misalignment or misplacement of the cutting instrument along the ideal tissue cutting plane.

As explained in detail above, the present disclosure incorporates knife assembly 70 which, when activated via the trigger knob 76, progressively and selectively divides the tissue along an ideal tissue plane in precise manner to effectively and reliably divide the tissue into two sealed halves with a tissue gap therebetween. The knife assembly 70 allows the user to quickly separate the tissue immediately after sealing without substituting a cutting instrument through a cannula or trocar port. As can be appreciated, accurate sealing and dividing of tissue is accomplished with the same forceps 10.

It is envisioned that knife blade 190 may also be coupled to the same or an alternative electrosurgical energy source to facilitate separation of the tissue along the tissue seal. Moreover, it is envisioned that the angle of the knife blade tip 192 may be dimensioned to provide more or less aggressive cutting angles depending upon a particular purpose. For example, the knife blade tip 192 may be positioned at an angle which reduces “tissue wisps” associated with cutting. More over, the knife blade tip 192 may be designed having different blade geometries such as serrated, notched, perforated, hollow, concave, convex etc. depending upon a particular purpose or to achieve a particular result. It is also contemplated that the forceps 10 may be activated in a monopolar mode to divide tissue after formation of a tissue seal.

Once the tissue is divided into tissue halves, the jaw members 110 and 120 may be opened by re-grasping the handles 30 a and 30 b moving each handle 30 a and 30 b outwardly relative to the housing 20. It is envisioned that the knife assembly 70 generally cuts in a progressive, unidirectional fashion (i.e., distally).

As best shown in FIGS. 3A-3C, the proximal portions of the jaw members 110 and 120 and the distal end 16 of shaft 12 may be covered by a resilient or flexible insulating material or boot 220 to reduce stray current concentrations during electrosurgical activation especially in the monopolar activation mode. More particularly, the boot 220 is flexible from a first configuration (See FIG. 3B) when the jaw members 110 and 120 are disposed in a closed orientation to a second expanded configuration (See FIGS. 3A and 3C) when the jaw members 110 and 120 are opened. As can be appreciated, when the jaw members 110 and 120 open, the boot flexes or expands at areas 220 a and 220 b to accommodate the movement of the proximal flanges 113 and 123. Further details relating to one envisioned insulating boot 220 are described with respect to commonly-owned and concurrently-filed U.S. Application Provisional Application Ser. No. 60/722,213 [Attorney docket No. 203-4546 (H-US-00237)] entitled “INSULATING BOOT FOR ELECTROSURGICAL FORCEPS”, the entire contents of which being incorporated by reference herein.

FIGS. 18-22C show one particularly useful embodiment of a safety lockout mechanism 255′ for use with a flex circuit 170′. Much like the above described safety lockout 255, lockout mechanism 255′ is disposed on handle 30 a′ at a point distal to trigger lockout 32′. This particular safety lockout 255′ is configured to extend normally to the longitudinal axis “A” as shown best in FIG. 18. Movement of handle 30 a′ towards housing 20 causes the safety lockout 255′ to move towards the housing 20 in a similar manner as described above. Safety lockout 255′ is configured to engage a safety switch 171′ of the flex circuit 170′ to allow activation only when handle 30 a′ (and, in turn, jaw members 110 and 120) is moved relative to housing 20 (i.e., both handles 30 a′ and 30 b are closed to grasp tissue).

As best shown in schematic illustration of FIG. 20, safety switch 171′ is designed as part of a circuit 400 such that circuit 400 remains open until the safety switch 171′ is activated. FIG. 21 shows the position of safety switch 171′ prior to and after assembly. More particularly, upon assembly, the safety switch 171′ is flexed into position (see phantom representation) by the top portion 20 a of housing 20 such that the distal portion of the safety switch 171′ is biased and wedged against an interior wall or ledge 173′ disposed within housing 20 b. It is envisioned that the safety switch 171′ will remain secured in place for the useful life of the forceps 10.

FIGS. 22A-22C show the activation sequence of the safety switch 171′. More particularly and as mentioned above, the safety switch 171′ when assembled (and when the handles 30 a′ and 30 b and jaws 110 and 120 are opened) is secured against an interior wall or ledge 173′ of housing 20 b as shown in FIG. 22A. Upon movement of the handle 30 a′ toward housing 20 b, safety lockout 255′ moves inwardly relative to the housing 20 b toward the safety switch 171′ as shown in FIG. 22B. As the handles 30 a′ and 30 b move toward the closed position (as described in detail above), the safety lockout 255′ engages the safety circuit 171′ to complete circuit 400 and allow selective activation of the forceps 10.

It is envisioned that the safety switch 171′ may be configured to allow both bipolar and monopolar activation once closed or configured in a more restrictive fashion, e.g., only permit one type of electrical activation at a time without re-setting the safety switch 171′ (i.e., opening and re-grasping the handles 30 a′ and 30 b, a separate toggle switch (not shown), etc.). Moreover, it is also envisioned that the safety switch 171′ may be configured to simply safeguard against the activation of one of the modes (i.e., the monopolar mode) depending upon a particular purpose and the other mode (i.e., the bipolar mode) is not restricted by the safety switch 171′.

From the foregoing and with reference to the various figure drawings, those skilled in the art will appreciate that certain modifications can also be made to the present disclosure without departing from the scope of the same. For example, it may be preferable to add other features to the forceps 10, e.g., an articulating assembly to axially displace the end effector assembly 100 relative to the elongated shaft 12.

It is also contemplated that the forceps 10 (and/or the electrosurgical generator used in connection with the forceps 10) may include a sensor or feedback mechanism (not shown) which automatically selects the appropriate amount of electrosurgical energy to effectively seal the particularly-sized tissue grasped between the jaw members 110 and 120. The sensor or feedback mechanism may also measure the impedance across the tissue during sealing and provide an indicator (visual and/or audible) that an effective seal has been created between the jaw members 110 and 120. Examples of such sensor systems are described in commonly-owned U.S. patent application Ser. No. 10/427,832 entitled “METHOD AND SYSTEM FOR CONTROLLING OUTPUT OF RF MEDICAL GENERATOR”, the entire contents of which being incorporated by reference herein.

Moreover, it is contemplated that the knife assembly 70 may include other types of recoil mechanisms which are designed to accomplish the same purpose, e.g., gas-actuated recoil, electrically-actuated recoil (i.e., solenoid), etc. It is also envisioned that the forceps 10 may be used to cut tissue without sealing. Alternatively, the knife assembly 70 may be coupled to the same or alternate electrosurgical energy source to facilitate cutting of the tissue.

Although the figures depict the forceps 10 manipulating an isolated vessel, it is contemplated that the forceps 10 may be used with non-isolated vessels as well. Other cutting mechanisms are also contemplated to cut tissue along the ideal tissue plane.

It is envisioned that the outer surface of the end effector assembly 100 may include a nickel-based material, coating, stamping, metal injection molding which is designed to reduce adhesion between the jaw members 110 and 120 with the surrounding tissue during activation and sealing. Moreover, it is also contemplated that the conductive surfaces 112 and 122 of the jaw members 110 and 120 may be manufactured from one (or a combination of one or more) of the following materials: nickel-chrome, chromium nitride, MedCoat 2000 manufactured by The Electrolizing Corporation of OHIO, inconel 600 and tin-nickel. The tissue conductive surfaces 112 and 122 may also be coated with one or more of the above materials to achieve the same result, i.e., a “non-stick surface”. As can be appreciated, reducing the amount that the tissue “sticks” during sealing improves the overall efficacy of the instrument.

One particular class of materials disclosed herein has demonstrated superior non-stick properties and, in some instances, superior seal quality. For example, nitride coatings which include, but not are not limited to: TiN, ZrN, TiAlN, and CrN are preferred materials used for non-stick purposes. CrN has been found to be particularly useful for non-stick purposes due to its overall surface properties and optimal performance. Other classes of materials have also been found to reducing overall sticking. For example, high nickel/chrome alloys with a Ni/Cr ratio of approximately 5:1 have been found to significantly reduce sticking in bipolar instrumentation. One particularly useful non-stick material in this class is Inconel 600. Bipolar instrumentation having sealing surfaces 112 and 122 made from or coated with Ni200, Ni201 (˜100% Ni) also showed improved non-stick performance over typical bipolar stainless steel electrodes.

While the drawings show one particular type of monopolar lockout or safety mechanism 255 for use with the presently disclosed forceps, FIGS. 18 and 19 show an alternative safety lockout mechanism which may be employed with the forceps 10.

While several embodiments of the disclosure have been shown in the drawings, it is not intended that the disclosure be limited thereto, as it is intended that the disclosure be as broad in scope as the art will allow and that the specification be read likewise. Therefore, the above description should not be construed as limiting, but merely as exemplifications of preferred embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the claims appended hereto. 

1. An endoscopic forceps, comprising: a housing having a shaft attached thereto, the shaft including a pair of jaw members disposed at a distal end thereof; a drive assembly disposed in the housing operable to move the jaw members relative to one another from a first position, wherein the jaw members are disposed in spaced relation relative to one another, to a second position, wherein the jaw members are closer to one another, for manipulating tissue; a pair of handles operatively connected to the drive assembly, the handles being movable relative to the housing to actuate the drive assembly to move the jaw members; each jaw member adapted to connect to a source of electrical energy such that the jaw members are capable of conducting energy for treating tissue; and a knife assembly operatively associated with the housing, the knife assembly being selectively actuatable to advance a knife through tissue disposed between the jaw members when the jaw members are disposed in the second position, the knife assembly including at least one safety mechanism to prevent damaging the knife upon selective actuation thereof.
 2. An endoscopic forceps according to claim 1 wherein the safety mechanism includes a mechanical fuse which fractures upon exertion of excessive force to actuate the knife assembly.
 3. An endoscopic forceps according to claim 2 wherein the knife assembly includes a pinion gear interdisposed between gear teeth and a track which cooperate to advance the knife distally through the jaw members, the mechanical fuse being operatively associated with at least one of the pinion gear, gear teeth and track.
 4. An endoscopic forceps according to claim 2 wherein the knife assembly includes a pinion gear interdisposed between gear teeth and a track which cooperate to advance the knife distally through the jaw members, the pinion gear including an axle which fractures upon excessive force to actuate the knife assembly.
 5. An endoscopic forceps according to claim 2 wherein the excessive force is at least about 9 lbf.
 6. An endoscopic forceps according to claim 4 wherein the excessive force is at least about 9 lbf.
 7. An endoscopic forceps according to claim 2 wherein the knife assembly includes a pinion gear interdisposed between gear teeth and a track which cooperate to advance the knife distally through the jaw members, the gear teeth being biased by a spring to return the knife assembly to an unactuated position.
 8. An endoscopic forceps according to claim 7 wherein upon the exertion of excessive force, the mechanical fuse fractures and the spring automatically returns the knife assembly to the unactuated position which, in turn, allows the user to move the handles relative to one another to release tissue.
 9. An endoscopic forceps according to claim 1 further comprising: a first switch disposed on the housing and being activatable to selectively deliver energy of a first electrical potential to at least one jaw member for treating tissue in a monopolar fashion; and a second switch disposed on the housing and being activatable to selectively deliver energy of a first electrical potential to one jaw member and selectively deliver energy of a second electrical potential to the other jaw member for treating tissue in a bipolar fashion.
 10. An endoscopic forceps according to claim 1 wherein at least one of the handles includes a knife lockout that prevents the knife assembly from being actuated when the jaw members are disposed in the second position.
 11. An endoscopic forceps according to claim 10 wherein the lockout mechanism includes a mechanical interface extending from at least one of the handles, the mechanical interface being dimensioned to impede movement of the knife assembly when the handles are disposed in a first open position relative to the housing and the mechanical interface being dimensioned to permit actuation of the knife assembly when the handles are disposed in a second position relative to the housing.
 12. An endoscopic forceps according to claim 1 wherein the forceps includes a monopolar lockout that prevents activation of the first switch when the jaw members are disposed in the first position.
 13. An endoscopic forceps according to claim 12 wherein the monopolar lockout includes a mechanical interface disposed on at least one of the handles that prevents activation of the first switch when the handles are disposed in a first position relative to the housing and permits activation of the first switch when the handles are disposed in a second position relative to the housing.
 14. An endoscopic forceps according to claim 12 wherein the monopolar lockout includes a pressure activated safety switch disposed in the housing and movement of the handles from a first position relative to the housing to a second position relative to the housing closes the pressure activated safety switch to allow activation of the first switch.
 15. An endoscopic forceps, comprising: a housing having a shaft attached thereto, the shaft including a pair of jaw members disposed at a distal end thereof; a drive assembly disposed in the housing operable to move the jaw members relative to one another from a first position, wherein the jaw members are disposed in spaced relation relative to one another, to a second position, wherein the jaw members are closer to one another, for manipulating tissue; a pair of handles operatively connected to the drive assembly, the handles being movable relative to the housing to actuate the drive assembly to move the jaw members; each jaw member adapted to connect to a source of electrical energy such that the jaw members are capable of conducting energy for treating tissue; and a switch disposed on the housing and being activatable to selectively deliver energy of a first electrical potential to at least one jaw member for treating tissue, the switch being operatively coupled to an intensity control mechanism disposed within the housing which is selectively adjustable to regulate the level of electrosurgical energy to at least one jaw member.
 16. An endoscopic forceps according to claim 15 wherein the intensity control mechanism is selectively adjustable in discreet increments.
 17. An endoscopic forceps according to claim 15 wherein the intensity control mechanism includes a first mechanical interface configured to engage a series of corresponding mechanical interfaces defined in the housing to regulate the level of electrosurgical energy in discreet increments.
 18. An endoscopic forceps according to claim 17 wherein the first mechanical interface includes a detent and the corresponding mechanical interfaces defined within the housing include recesses.
 19. An endoscopic forceps according to claim 18 wherein the intensity control mechanism includes a second mechanical interface that cooperates with the detent to mechanically engage a circuit board disposed within the housing at discreet locations when the detent engages a corresponding one of the series of recesses.
 20. An endoscopic forceps according to claim 18 wherein the detent is disposed in a cantilevered fashion atop the intensity control mechanism.
 21. An endoscopic forceps according to claim 15 wherein the intensity control is positioned atop a railway defined within the housing.
 22. An endoscopic forceps, comprising: a housing having a shaft attached thereto, the shaft including a pair of jaw members disposed at a distal end thereof; a drive assembly disposed in the housing operable to move the jaw members relative to one another from a first position, wherein the jaw members are disposed in spaced relation relative to one another, to a second position, wherein the jaw members are closer to one another, for manipulating tissue; a pair of handles operatively connected to the drive assembly, the handles being movable relative to the housing to actuate the drive assembly to move the jaw members; each jaw member adapted to connect to a source of electrical energy such that the jaw members are capable of conducting energy for treating tissue; a switch disposed on the housing and being activatable to selectively deliver energy of a first electrical potential to at least one jaw member for treating tissue; and first and second toggle links which operatively connect each one of the pair of handles to the drive assembly, each of the toggle links including first and second anchoring elements, the first anchoring element operatively engaging the handle and the second anchoring element operatively engaging the drive assembly.
 23. An endoscopic forceps according to claim 22 wherein the first and second anchoring elements each include a pair of double tangs which operatively engage the handle and the drive assembly, respectively, in a snap-fit manner.
 24. An endoscopic forceps according to claim 23 wherein each pair of double tangs is tapered.
 25. An endoscopic forceps according to claim 24 wherein each pair of double tangs includes a step at a proximal end thereof for seating each pair of double tangs within a respective aperture defined within the handle and the drive assembly.
 26. An endoscopic forceps according to claim 23 wherein each pair double tangs includes a slot defined therebetween, the slots being oriented such that the greatest cross sectional area of the double tangs offsets an applied load on the forceps. 